tert-Butyl (S)-2-methyl-4,6-dioxopiperidine-1-carboxylate CAS 653589-14-1

Purity 97%+In StockPharmaceutical Standards
CAS No.653589-14-1
Molecular FormulaC11H17NO4
Molecular Weight227.26 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-Butyl (S)-2-methyl-4,6-dioxopiperidine-1-carboxylate CAS 653589-14-1 chemical structure

Description

tert-Butyl (S)-2-methyl-4,6-dioxopiperidine-1-carboxylate (C11H17NO4) contains an amino-acid-derived structure, an amide group, a hydroxyl group, an ether linkage. It is notably hygroscopic, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

CATO supplies tert-Butyl (S)-2-methyl-4,6-dioxopiperidine-1-carboxylate (CAS 653589-14-1), a certified reference material (molecular formula C11H17NO4, MW 227.26 g/mol) for analytical method development and quality control.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

CATO manufactures tert-Butyl (S)-2-methyl-4,6-dioxopiperidine-1-carboxylate under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC11H17NO4
Molecular Weight227.26 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, ethanol, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1985
Nitrogen Atoms1

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